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rs397508024

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508024(-;-)
Make rs397508024(-;A)
Make rs397508024(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379752
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508024
ebirs397508024
HLIrs397508024
Exacrs397508024
Varsomers397508024
Maprs397508024
PheGenIrs397508024
hapmaprs397508024
1000 genomesrs397508024
hgdprs397508024
ensemblrs397508024
gopubmedrs397508024
geneviewrs397508024
scholarrs397508024
googlers397508024
pharmgkbrs397508024
gwascentralrs397508024
openSNPrs397508024
23andMers397508024
23andMe allrs397508024
SNP Nexus

SNPshotrs397508024
SNPdbers397508024
MSV3drs397508024
GWAS Ctlgrs397508024
Max Magnitude0
ClinVar
Risk rs397508024(A;A)
Alt rs397508024(A;A)
Reference rs397508024(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953889dupA
CLNSRC ClinVar
CLNACC RCV000045672.2,